Job Title- Sr. Technical Writer
Location- Acton, MA 01720 (Hybrid)
Duration- 3 months Assignment

Position Overview:

The Sr Technical Writer will collaborate with QMS Process Owners to establish top-level Standard Operating Procedures (SOPs) for multiple QMS Processes.

Responsibilities:

• Work with various subject matter experts across multiple departments including but not limited to Quality Systems, Document Control, Design & Development, Regulatory, Post Market, Purchasing, Supplier Quality and Production Controls.
• Develop top-level SOPs which include documenting applicable regulatory requirements & standards, incorporating Business requirements, and defining and documenting key Inputs and Outputs.
• Evaluate and update existing SOPs to ensure compliance.

 
Minimum Requirements:

• A minimum of 5 years’ technical writing experience, preferably developing top-level procedures.
• Bachelor's or equivalent experience.
• Minimum of 3 years of experience in Medical Device manufacturing.
• Strong organizational and written communication skills.
• Proficient in all MS Office applications.
• Excellent written English skills.
• Excellent verbal interpersonal skills.
• Excellent attention to detail and organizational skills.
• Eagerness and aptitude to learn new technologies quickly.
• Ability to contribute broadly to documentation structure and design.
• Able to handle high workload, multiple responsibilities, and tight deadlines.
• Motivation to succeed while working independently.

 
Preferred Skills and Competencies:

• Previous experience authoring and publishing controlled documentation.
• Experience working within a PLM system (Arena preferred).
• Strong planning, organization, and multitasking skills.

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 57.00/hr.